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Deep sequencing reveals increased DNA methylation in chronic rat epilepsy

Epilepsy is a frequent neurological disorder, although onset and progression of seizures remain difficult to predict in affected patients, irrespective of their epileptogenic condition. Previous studies in animal models as well as human epileptic brain tissue revealed a remarkably diverse pattern of...

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Autores principales: Kobow, Katja, Kaspi, Antony, Harikrishnan, K. N., Kiese, Katharina, Ziemann, Mark, Khurana, Ishant, Fritzsche, Ina, Hauke, Jan, Hahnen, Eric, Coras, Roland, Mühlebner, Angelika, El-Osta, Assam, Blümcke, Ingmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825532/
https://www.ncbi.nlm.nih.gov/pubmed/24005891
http://dx.doi.org/10.1007/s00401-013-1168-8
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author Kobow, Katja
Kaspi, Antony
Harikrishnan, K. N.
Kiese, Katharina
Ziemann, Mark
Khurana, Ishant
Fritzsche, Ina
Hauke, Jan
Hahnen, Eric
Coras, Roland
Mühlebner, Angelika
El-Osta, Assam
Blümcke, Ingmar
author_facet Kobow, Katja
Kaspi, Antony
Harikrishnan, K. N.
Kiese, Katharina
Ziemann, Mark
Khurana, Ishant
Fritzsche, Ina
Hauke, Jan
Hahnen, Eric
Coras, Roland
Mühlebner, Angelika
El-Osta, Assam
Blümcke, Ingmar
author_sort Kobow, Katja
collection PubMed
description Epilepsy is a frequent neurological disorder, although onset and progression of seizures remain difficult to predict in affected patients, irrespective of their epileptogenic condition. Previous studies in animal models as well as human epileptic brain tissue revealed a remarkably diverse pattern of gene expression implicating epigenetic changes to contribute to disease progression. Here we mapped for the first time global DNA methylation patterns in chronic epileptic rats and controls. Using methyl-CpG capture associated with massive parallel sequencing (Methyl-Seq) we report the genomic methylation signature of the chronic epileptic state. We observed a predominant increase, rather than loss of DNA methylation in chronic rat epilepsy. Aberrant methylation patterns were inversely correlated with gene expression changes using mRNA sequencing from same animals and tissue specimens. Administration of a ketogenic, high-fat, low-carbohydrate diet attenuated seizure progression and ameliorated DNA methylation mediated changes in gene expression. This is the first report of unsupervised clustering of an epigenetic mark being used in epilepsy research to separate epileptic from non-epileptic animals as well as from animals receiving anti-convulsive dietary treatment. We further discuss the potential impact of epigenetic changes as a pathogenic mechanism of epileptogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00401-013-1168-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-38255322013-11-21 Deep sequencing reveals increased DNA methylation in chronic rat epilepsy Kobow, Katja Kaspi, Antony Harikrishnan, K. N. Kiese, Katharina Ziemann, Mark Khurana, Ishant Fritzsche, Ina Hauke, Jan Hahnen, Eric Coras, Roland Mühlebner, Angelika El-Osta, Assam Blümcke, Ingmar Acta Neuropathol Original Paper Epilepsy is a frequent neurological disorder, although onset and progression of seizures remain difficult to predict in affected patients, irrespective of their epileptogenic condition. Previous studies in animal models as well as human epileptic brain tissue revealed a remarkably diverse pattern of gene expression implicating epigenetic changes to contribute to disease progression. Here we mapped for the first time global DNA methylation patterns in chronic epileptic rats and controls. Using methyl-CpG capture associated with massive parallel sequencing (Methyl-Seq) we report the genomic methylation signature of the chronic epileptic state. We observed a predominant increase, rather than loss of DNA methylation in chronic rat epilepsy. Aberrant methylation patterns were inversely correlated with gene expression changes using mRNA sequencing from same animals and tissue specimens. Administration of a ketogenic, high-fat, low-carbohydrate diet attenuated seizure progression and ameliorated DNA methylation mediated changes in gene expression. This is the first report of unsupervised clustering of an epigenetic mark being used in epilepsy research to separate epileptic from non-epileptic animals as well as from animals receiving anti-convulsive dietary treatment. We further discuss the potential impact of epigenetic changes as a pathogenic mechanism of epileptogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00401-013-1168-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-09-05 2013 /pmc/articles/PMC3825532/ /pubmed/24005891 http://dx.doi.org/10.1007/s00401-013-1168-8 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Kobow, Katja
Kaspi, Antony
Harikrishnan, K. N.
Kiese, Katharina
Ziemann, Mark
Khurana, Ishant
Fritzsche, Ina
Hauke, Jan
Hahnen, Eric
Coras, Roland
Mühlebner, Angelika
El-Osta, Assam
Blümcke, Ingmar
Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title_full Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title_fullStr Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title_full_unstemmed Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title_short Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
title_sort deep sequencing reveals increased dna methylation in chronic rat epilepsy
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825532/
https://www.ncbi.nlm.nih.gov/pubmed/24005891
http://dx.doi.org/10.1007/s00401-013-1168-8
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